Canonical Allele Identifier: CA348658696

Gene: CXCR4

Linked Data

• dbSNP Id: rs2104917278
• MyVariant Identifiers: chr2:g.136872989G>A (hg19) ; chr2:g.136115419G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.136115419G>A , CM000664.2:g.136115419G>A	GRCh38
NC_000002.11:g.136872989G>A , CM000664.1:g.136872989G>A	GRCh37
NC_000002.10:g.136589459G>A	NCBI36
NG_011587.1:g.7737C>T , LRG_51:g.7737C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696136.1:c.497C>T	ENSP00000512428.1:p.Pro166Leu
ENST00000696137.1:c.464C>T	ENSP00000512429.1:p.Pro155Leu
ENST00000696152.1:c.464C>T	ENSP00000512443.1:p.Pro155Leu
ENST00000696228.1:c.497C>T	ENSP00000512494.1:p.Pro166Leu
ENST00000241393.4:c.509C>T MANE Select	ENSP00000241393.3:p.Pro170Leu
ENST00000241393.3:c.509C>T	ENSP00000241393.3:p.Pro170Leu
ENST00000409817.1:c.521C>T	ENSP00000386884.1:p.Pro174Leu
ENST00000466288.1:n.703C>T
NM_001008540.1:c.521C>T	NP_001008540.1:p.Pro174Leu
NM_003467.2:c.509C>T , LRG_51t1:c.509C>T	NP_003458.1:p.Pro170Leu
NM_001008540.2:c.521C>T	NP_001008540.1:p.Pro174Leu
NM_001348056.1:c.722C>T	NP_001334985.1:p.Pro241Leu
NM_001348059.1:c.608C>T	NP_001334988.1:p.Pro203Leu
NM_001348060.1:c.464C>T	NP_001334989.1:p.Pro155Leu
NM_001348056.2:c.722C>T	NP_001334985.1:p.Pro241Leu
NM_001348059.2:c.608C>T	NP_001334988.1:p.Pro203Leu
NM_001348060.2:c.464C>T	NP_001334989.1:p.Pro155Leu
NM_003467.3:c.509C>T MANE Select	NP_003458.1:p.Pro170Leu